CDKL5 Mutations in Boys With Encephalopathy and Early-Onset Intractable Epilepsy
Clinical and EEG data of 3 Italian boys (ages 3, 9, and 13 years) with severe early-onset encephalopathy, mental retardation, facial dysmorphisms, and intractable epilepsy were found to carry missense mutations in the CDKL5 gene, in a report from Troina, Italy.
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| Format: | Book |
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Pediatric Neurology Briefs Publishers,
2008-10-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | Clinical and EEG data of 3 Italian boys (ages 3, 9, and 13 years) with severe early-onset encephalopathy, mental retardation, facial dysmorphisms, and intractable epilepsy were found to carry missense mutations in the CDKL5 gene, in a report from Troina, Italy. |
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| Item Description: | 1043-3155 2166-6482 10.15844/pedneurbriefs-22-10-5 |